rs1592488602
- Uncertain significance
Your Genotype
Sign InDescription
Reference Allele
G
Alternative Allele
A
Chromosome
12
Location
32633559
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_001370298.3(FGD4):c.2183G>A (p.Trp728Ter)
Allele
A
Clinical Significance
Uncertain significance